{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "East Walpole",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88768",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc",
      "address_1": "333 Coney St",
      "address_2": "N/A",
      "postal_code": "02032-1516",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AK, CA, CO, DC, GA, IL, ME, NC, NV, NY, OR, PA, PR, VA and VI.",
      "recall_number": "Z-0196-2022",
      "product_description": "ADVIA Centaur SARS-CoV-2 Antigen Assay (100 Test Kit), SMN # 11207866",
      "product_quantity": "261 kits",
      "reason_for_recall": "Data provided in the Emergency Use Authorization (EUA) submission was insufficient to determine that the assays were adequately validated for the intended use.",
      "recall_initiation_date": "20210922",
      "center_classification_date": "20211103",
      "termination_date": "20220802",
      "report_date": "20211110",
      "code_info": "Lot # 44990001, Exp. Date 2021-10-07,  UDI # (01)00630414611747(10)44990001(17)20211007.  Lot # 60408003, Exp. Date 2021-11-12,  UDI # (01)00630414611747(10)60408003(17)20211112."
    }
  ]
}